HealthLawProf Blog

Editor: Katharine Van Tassel
Concordia University School of Law

Saturday, September 20, 2008

Drug Label, Maimed Patient and Crucial Test for Justices

The New York Times reports that the Supreme Court will hear arguments about whether plaintiffs have the right to sue when the products that hurt them had met federal standards.  Adam Liptak writes,

Gavel4When Diana Levine starts talking about her rock ’n’ roll days, she plays a little air guitar, mimicking the way she used to handle her electric bass in bands like the Re-Bops and Duke and the Detours. But Ms. Levine is missing much of her right arm, which was amputated below the elbow after a medical disaster.

She sits at her kitchen table, strumming an imaginary guitar with a phantom hand.

In November, the Supreme Court will hear arguments about whether Ms. Levine may keep more than $6 million that a Vermont jury ordered Wyeth, a pharmaceutical company, to pay her for failing to warn her adequately about the risks of one of its drugs. The case, the latest in a brisk parade of similar ones, will help define the contours of a signature project of the Roberts court.

In legal jargon, the cases concern “pre-emption,” a doctrine that can bar injured consumers like Ms. Levine from suing in state court when the products that hurt them had met federal standards. The issue is less boring and more consequential than it sounds, and Ms. Levine’s case is shaping up to be the most important business case of the term.

“Federal pre-emption is the fiercest battle in products liability law today,” said Catherine M. Sharkey, a law professor at New York University. “The court clearly recognizes this, as it has agreed to hear so many cases and seems eager to give clarity to what has been, to date, an undisputably muddled area of law.”

A second pre-emption case, this one concerning cigarette labels, is scheduled for the first argument of the new term, on Oct. 6.

Business groups, often supported by the Bush administration, have vigorously pursued pre-emption arguments, hoping to build a barrier against many kinds of injury suits. Plaintiffs’ lawyers oppose broad pre-emption doctrines, saying they short-circuit valid claims arising from terrible injuries.

Ms. Levine is a trim, elegant 62-year-old who now favors three-quarter length sleeves, just long enough to cover what remains of her right arm. But she gestures enthusiastically with both arms, and she retains a playful side.

Her house is jammed with whimsical toys — a papier-mâché giraffe, an enormous telephone receiver. In the control room of her recording studio, there is a copy of “Hand, Hand, Fingers, Thumb,” a children’s book. “It’s just sarcasm,” she explained.

In the spring of 2000, suffering from a migraine, Ms. Levine visited a clinic near here for a treatment she had received many times: Demerol for the pain and Wyeth’s drug Phenergan for nausea.

“Nothing wrong with either drug,” Ms. Levine said. “They’re both safe when given the right way.”

But if Phenergan is exposed to arterial blood, it causes swift and irreversible gangrene. For that reason, it is typically administered by intramuscular injection. According to Ms. Levine’s lawyers, using an intravenous drip is almost entirely safe as well.

This time, though, a physician’s assistant used a third method. She injected the drug into what she thought was a vein, a method known as “IV push.” But the assistant apparently missed.

In the following weeks, Ms. Levine’s hand and forearm turned purple and then black, and they were amputated in two stages.

The drug’s label, approved by the Food and Drug Administration, had warned that “inadvertent intra-arterial injection” can result in “gangrene requiring amputation.” But it did not rule out administration of the drug by IV push.

Ms. Levine said no one had discussed the risks of IV push with her, or the only benefit generally associated with intravenous administration — “more potent and expeditious antinausea relief,” in the words of Wyeth’s brief.

“The benefit-risk is just outrageously ridiculous,” Ms. Levine said. “Any child could figure this out.”

Faster nausea relief, she said, is not worth the risk of losing an arm.

Ms. Levine settled a lawsuit against the clinic, and she went to trial in Montpelier, not far from here, against Wyeth. She said Wyeth should have added a stronger warning to the label that the F.D.A. had approved.

“All they had to do,” Ms. Levine said, “was change the label and say, ‘Don’t give it this way.’ ”

Lawyers for Wyeth said that was not an option, at least in the absence of new information. “Wyeth could not change Phenergan’s labeling to comply with Vermont law without violating federal law,” they wrote in a brief. Ms. Levine’s lawyers disagreed, saying that tougher warnings were always permissible.

Continue reading "Drug Label, Maimed Patient and Crucial Test for Justices"

| Permalink

TrackBack URL for this entry:

Listed below are links to weblogs that reference Drug Label, Maimed Patient and Crucial Test for Justices :


Preemption complies with the Supremacy Clause.

At the policy level, it promotes commerce by setting out a single national standard.

It helps patients by reducing the incentive to avoid or to seek out the consumers of a state depending on the attitudes of judges in the pockets of local, rent seeking litigators. Phenergan will get more expensive or even get withdrawn to the detriment of millions of future users, so that this unseemly victim and her rent seeking lawyers can score an unjust windfall.

Beyond that, preemption preserves the procedural due process right of notice, held to be a right of civil defendants in several Supreme Court cases.

As to the validity of the jury verdict? Every party in that trial, all the way up to defense experts, was subject to outcome bias. This bias has yet to be used as a defense, to my knowledge. However, it violates the defendant's right to a fair hearing as much as any bias, such as racial animus. It induces the same quality and quantity of animus in the jury as racial hatred.

If I were the court, I would evade the issue. Remand for a medmal trial. The medication was put into an artery that flows toward the small body part, instead of in a vein, that flows back to the heart and the rest of the body, to be diluted. A nurse made a mistake. The plaintiff is being used with public freak show vulgarity to go after the wrong party, but one with deep pockets.

As a patient, I want those deep pockets to go to research, and future medications. I object to their enriching rent seeking enemies of clinical care, including this victim.

Posted by: Supremacy Claus | Sep 21, 2008 8:04:30 AM

Post a comment